Cosmetic recalls

ORL Labs is recalling six ORL Organic Oral Care kids' and adult toothpaste and mouthwash products sold nationwide. The FDA's sampling found progesterone, estradiol, or DHEA (a hormone) in the products, which the company says is due to cross-contamination. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·ORL Labs6 products

BioMed Laboratories is recalling three Tychasis Coats products: aloe lotion (allantoin 0.5%), aloe creme (allantoin 0.5%) and aloe liniment (methyl salicylate 10%), in several bottle and jar sizes. The FDA reports that stability test results for viscosity and appearance did not align with the established specifications. The products were distributed in Texas only, and no injuries have been reported.

Moderate·FDA·Nov 2, 2026·BioMed Laboratories3 products

ABC Compounding Co. is recalling Handtastic Foamy Mango Antiseptic Foam Soap Hand & Body Wash, sold by Momar Incorporated. The FDA classified the recall as Class II because the product was made in a way that did not meet federal manufacturing standards (CGMP). About 10,908 bottles were distributed nationwide, and no injuries have been reported.

Moderate·FDA·Oct 27, 2026·ABC Compounding19 products

Pritam International Private Limited issued a recall of Brush Buddies Crayola Silly Scents Anticavity Fluoride Toothpaste (Bubble Gum flavor, 4.0 oz) due to Current Good Manufacturing Practice (CGMP) deviations during production. Approximately 320,232 tubes across multiple lot numbers are affected and have been distributed nationwide.

Moderate·FDA·Oct 19, 2026·PRITAM INTERNATIONAL PRIVATE LIMITED17 products

DANALVIG LLC is recalling two skin whitening creams, Orbi 20 Whitening Cream and Omni Gold Anti-Marks Cream Extra Brightening, sold nationwide through eBay. FDA analysis found the products contain mercury, and both are made by White Gold International in Lahore, Pakistan. No injuries have been reported.

Serious·FDA·Oct 14, 2026·DANALVIG LLC2 products

MENOW Sunscreen Pressed Powder SPF35 PA+++ was manufactured in ways that do not meet U.S. cosmetic manufacturing standards (cGMP deviations). The affected product was distributed in California only. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Shantou Qiwei

Testing found that THE ONE SPF 50 Invisible Sunscreen Gel sachets may not provide the SPF 50 sun protection stated on the label. The affected product was distributed nationwide in the U.S. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Allies4 products

Schwarzkopf Professional Osis Grip extra strong mousse in 6.76 fl. oz aluminum cans may leak under pressure due to a packaging defect, creating a risk of explosion. The affected product was sold to salons and retailers across the U.S. Henkel learned of the issue through one customer complaint and two salon reports, with one instance of hand bruising reported.

Serious·FDA·Aug 11, 2026·Schwarzkopf Professional

Kao USA recalled select lots of Oribe Serene Scalp Densifying Shampoo (8.5 oz and 33.8 oz) made between February 21–26, 2026 after detecting Pluralibacter gergoviae bacteria. People with weakened immune systems may be at higher risk of infection.

Moderate·FDA·Jul 1, 2026·Kao

Target is recalling Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes after FDA testing found harmful bacteria (Burkholderia cepacia complex and Burkholderia gladioli) in product samples. Some customers also reported discoloration. These bacteria can cause serious infections, especially in newborns and infants with developing immune systems.

Serious·FDA·Jun 4, 2026·Target

Pharmacal recalled one lot of MG217 Multi-Symptom Treatment Cream & Skin Protectant Eczema Cream (6oz tube, lot 1024088) because it was found to contain Staphylococcus aureus bacteria. The contaminated product could cause infections ranging from localized skin infections to serious conditions like sepsis, especially in people with weakened immune systems or compromised skin. No illnesses have been reported so far.

Moderate·FDA·May 8, 2026·Pharmacal

Island Kinetics, Inc. (d.b.a. CoValence Laboratories) is recalling specific lots of Skin Script Blemish Spot Treatment because the product failed stability testing. This means the product may not maintain its intended strength or safety over time. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·CoValence Laboratories

Owen Biosciences is recalling four benzoyl peroxide acne products over possible benzene contamination, a chemical linked to cancer with long-term exposure. The products are FHF Farmhouse Fresh Midnight Clearing Night Lotion, HydroPeptide Clear Alliance Serum, and two SLMD (Sandra Lee MD) acne products, distributed by Skin PS Brands. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·Owen Biosciences4 products

Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.

Moderate·FDA·Apr 9, 2026

Carmex lip balm products distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity. The products may have been affected by insanitary conditions at their distribution center. This recall affects jars and tubes sold nationwide.

Moderate·FDA·Jan 21, 2026·Gold Star Distribution27 products

ORL Labs recalled ORL Kids Natural Toothpaste in Bubblegum Flavor due to deviations from manufacturing quality standards (cGMP). The affected product is Lot #250520P4 with expiration date 05/27, distributed in Arizona. No injuries have been reported.

Moderate·FDA·Jan 14, 2026·Signature Formulations2 products

CA Botana is recalling 14 skin care products, including mineral sunscreens, tinted moisturizers, acne creams, and pain relief gels. The products were sold under several brands, including Doctor D. Schwab, Gabriel, Karina, Sugared+Bronzed, Elixir by Coco March, CLEARSTEM, Dr. Bump, and Sea Enzyme. The recall covers manufacturing that did not meet FDA quality standards, and it applies to products distributed in CA, CO, FL, PR, and WA. No injuries have been reported.

Moderate·FDA·Dec 3, 2025·CA Botana14 products

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

FDA·Nov 26, 2025·DermaRite18 products